Structure–activity relationships of various amino-hydroxy-benzenesulfonic acids and sulfonamides as tyrosinase substrates

Rescigno, Antonio;Bruyneel, Frédéric;Padiglia, Alessandra;Sollai, Francesca;Sanjust, Enrico;et.al.
(2011) BBA - General Subjects — p. 799-807 (2011)

Files

BBAvol18102011pp799-807PUBLIE.pdf
  • Restricted Access
  • Adobe PDF
  • 1.3 MB

Details

Authors
  • Rescigno, AntonioUniversità di Cagliari
    Author
  • Bruyneel, FrédéricUCLouvain
    Author
  • Padiglia, AlessandraUniversità di Cagliari
    Author
  • Sollai, FrancescaUniversità di Cagliari
    Author
  • Marchand-Brynaert, JacquelineUCLouvain
    Author
  • Sanjust, EnricoUniversità di Cagliari
    Author
Show more
Abstract
o-Aminophenols have been long recognised as tyrosinase substrates. However their exact mode of interaction with the enzyme's active site is unclear. Properly vic-substituted o-aminophenols could help gain some insight into tyrosinase catalytic mechanism. Methods: Eight vic-substituted o-aminophenols belonging to two isomeric series were systematically evaluated as tyrosinase substrates and/or activators and/or inhibitors, by means of spectrophotometric techniques and HPLC-MS analysis. Some relevant kinetic parameters have also been obtained. Results: Four o-aminophenolic compounds derived from 3-hydroxyorthanilic acid (2-amino-3-hydroxybenzenesulfonic acid) and their four counterparts derived from the isomeric 2-hydroxymetanilic acid (3-amino-2- hydroxybenzenesulfonic acid) were synthesised and tested as putative substrates for mushroom tyrosinase. While the hydroxyorthanilic derivatives were quite inactive as both substrates and inhibitors, the hydroxymetanilic compounds on the contrary all acted as substrates for the enzyme, which oxidised them to the corresponding phenoxazinone derivatives. General significance: Based on the available structures of the active sites of tyrosinases, the different affinities of the fourmetanilic derivatives for the enzyme, and their oxidation rates,we propose a new hypothesis regarding the interaction between o-aminophenols and the active site of tyrosinase that is in agreement with the obtained experimental results.
Affiliations

Citations

Rescigno, A., Bruyneel, F., Padiglia, A., Sollai, F., Salis, A., Marchand-Brynaert, J., & Sanjust, E. (2011). Structure–activity relationships of various amino-hydroxy-benzenesulfonic acids and sulfonamides as tyrosinase substrates. BBA - General Subjects, 799-807. https://doi.org/10.1016/j.bbagen.2011.05.002 (Original work published 2011)